Canonical Allele Identifier: PA2827986598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487051
ClinVar RCV Id: RCV000567763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1540Phe
CA16031733
NM_001354900.2:c.4619C>T